Hierarchically Structured Porous Silica Spheres by Microemulsion/Vesicle Templating for Hydrodesulfurization of Fluid Catalytic Cracking Diesel

A series of hierarchically structured porous silica sphere (HSPSS) materials are successfully fabricated by a facile, one‐step microemulsion/vesicle bimodal method in a multicomponent microemulsion system of P123/n‐butanol/1,3,5‐trimethylbenzene/KCl/H₂O (surfactant/cosurfactant/oil/salt/water). The pore structures of the obtained HSPSS products consist of mesocellular foam and mesostructured vesicles. In contrast to the traditional porous silica materials the new structures combine two separate, distinct mesophases with different‐sized mesovoids in a single porous sphere. Moreover, the proportion of every mesophase in obtained HSPSS can be easily adjusted by tuning the initially added amount of n‐butanol or KCl in this multicomponent microemulsion system. When the molar ratio of KCl/tetraethoxysilane is 2.15, the obtained HSPSS material is turned into uniform mesostructured vesicle silica spheres, which consist of many small diameter vesicle particles. The hydrodesulfurization (HDS) activity of fluid catalytic cracking diesel over the HSPSS was tested. HSPSS‐0.75‐1.43 catalyst support with multiple mesoporous structures shows the highest HDS efficiency (98.5%) among all the studied catalysts.     

基于RFM的机载余度计算机软件快速测试平台

现代飞机普遍采用电传飞行控制系统,飞行控制计算机是该系统的核心。为了提升飞控计算机的可靠性,普遍采用余度技术构建余度飞控计算机,该计算机由多个通道构成,每个通道有一个CPU,互相构成备份。但是,这给飞控计算机的软件调试和测试带来的巨大的困难,因为各个通道的机载软件之间相互同步、通信和交叉监控,必须并行调试和测试,这就造成了机载软件调试和测试的滞后,必须等待真实的飞控计算机开发出来之后才能开展工作。本文提出了一种基于RFM(反射内存)的余度计算机快速原型测试平台设计方法。该平台使用商用货架产品构成余度计算机的多个冗余通道,使用RFM模拟多通道间的通信、同步过程,通过对底层驱动封装实现硬件故障模拟和余度功能模拟,方便实现软件调试和从性能、功能测试,大大提高了开发效率,减少了研制周期。     

Superior effect of a pi-acceptor ligand (phosphine-electron-deficient olefin ligand) in the Negishi coupling involving alkylzinc reagents

Palladium-catalyzed Negishi cross-coupling involving primary and secondary alkyls, even in the presence of beta-H, can be achieved at ambient temperature using chelating ligands containing a phosphine and an electron-deficient olefin. The superior effects of the ligands were shown not only in the desired cross-coupling product yields but also in the fast reaction at mild conditions. This reaction has been also scaled up to 50 g in 0.005 mol % catalyst (20,000 TONs) at room temperature.     

Organo[2-(hydroxymethyl)phenyl]dimethylsilanes as mild and reproducible agents for rhodium-catalyzed 1,4-addition reactions

Stable and reusable tetraorganosilicon reagents, alkenyl-, aryl-, and silyl[2-(hydroxymethyl)phenyl]dimethylsilanes, undergo 1,4-addition reactions to alpha,beta-unsaturated carbonyl acceptors under mild rhodium-catalysis. The reaction tolerates a diverse range of functional groups and is applicable to gram-scale synthesis. Use of a chiral diene ligand allows the achievement of the corresponding enantioselective transformations using the tetraorganosilicon reagents, providing the silicon-based approach to optically active ketones and substituted piperidones that serve as synthetic intermediates of pharmaceuticals. A rhodium alkoxide species is suggested to be responsible for a transmetalation step on the basis of the observed kinetic resolution of a racemic chiral phenylsilane in the enantioselective 1,4-addition reaction under the rhodium-chiral diene catalysis.     

Error estimation of a kind of rational spline

This paper deals with the approximation properties of a kind of rational spline with linear denominator when the function being interpolated is C³$C^3$ in an interpolating interval. Error estimate expressions of interpolating functions are derived, convergence is established, the optimal error coefficient, _ci$c_i$, is proved to be symmetric about the parameters of the rational interpolation and it is bounded. Finally, the precise jump measurements of the second derivatives of the interpolating function at the knots are given.